Enhanced far infrared emissivity, UV protection and near-infrared shielding of polypropylene composites via incorporation of natural mineral for functional fabric development.

Far infrared radiation in the range of 4-20 µm has been showed to have biological and health benefits to the human body. Therefore, incorporating far-infrared emissivity additives into polymers and/or fabrics hold promise for the development of functional textiles. In this study, we incorporated nine types of natural minerals into polypropylene (PP) film and examined their properties to identify potential candidates for functional textiles and apparels. The addition of 2% mineral powders into PP film increased the far-infrared emissivity (5-14 µm) by 7.65%-14.48%. The improvement in far-infrared emissivity within the range of 5-14 µm, which overlaps with the peak range of human skin radiation at 8-14 µm, results in increased absorption efficiency, and have the potential to enhance thermal and biological effects. Moreover, the incorporation of mineral powders in PP films exhibited favorable ultraviolet (UV) protection and near-infrared (NIR) shielding properties. Two films, specifically those containing red ochre and hematite, demonstrated excellent UV protection with a UPF rating of 50+ and blocked 99.92% and 98.73% of UV radiation, respectively. Additionally, they showed 95.2% and 93.2% NIR shielding properties, compared to 54.1% NIR shielding properties of PP blank films. The UV protection and NIR shielding properties offered additional advantages for the utilization of polymer composite with additives in the development of sportswear and other outdoor garments. The incorporation of minerals could absorb near-IR radiation and re-emit them at longer wavelength in the mid-IR region. Furthermore, the incorporation of minerals significantly improved the heat retention of PP films under same heat radiation treatment. Notably, films with red ochre and hematite exhibited a dramatic temperature increase, reaching 2.5 and 3.2 times the temperature increase of PP films under same heat radiation treatment, respectively (46.8 °C and 59.9 °C higher than the temperature increase of 20.9 °C in the PP film). Films with additives also demonstrated lower thermal effusivity than PP blank films, indicating superior heat insulation properties. Therefore, polypropylene films with mineral additives, particularly those containing red ochre and hematite, showed remarkable heat capacity, UV-protection, NIR-shielding properties and enhanced far infrared emissivity, making them promising candidates for the development of functional textiles.

Bacterial cellulose impregnated with andaliman (Zanthoxylum acanthopodium) microencapsulation as diabetic wound dressing.

Diabetic foot ulcer (DFU) is a common complication of diabetes mellitus which can cause infection, amputation and even death. One of many treatments that can be applied to support the DFU healing processes is by using wound dressings. Bacterial cellulose (BC) is a good material to be used as a wound dressing. However, some of the limitations of BC to be applied as wound dressing are does not possess antibacterial properties and support the healing process. Andaliman (Zanthoxylum acanthopodium) is known to have antioxidant, antibacterial and anti-inflammatory abilities that can support BC as a wound dressing. This research focused on the manufacture of BC/Z. acanthopodium microencapsulated wound dressing composites and evaluate their potential as a DFU wound dressing with a variety of gelatin composition in microencapsulation. The results of FTIR and SEM analysis showed that the Z. acanthopodium impregnation process in BC was successful. The variation of gelatine that used in microencapsulation affected the morphological and effectiveness of the wound dressing. However, overall, the wound dressings showed good antibacterial effect on E. coli and S. aureus bacteria and accelerating the wound closure process 8 times faster (BCAMc12) on the 17th day compared to wounds that did not receive any treatment.

Photocatalytic Degradation of Methylene Blue Using N-Doped ZnO/Carbon Dot (N-ZnO/CD) Nanocomposites Derived from Organic Soybean.

This study reports on successful synthesis of carbon dots (CDs), nitrogen-doped zinc oxide (N-ZnO), and N-ZnO/CD nanocomposites as photocatalysts for degradation of methylene blue. The first part was the synthesis of CDs utilizing a precursor from soybean and ethylenediamine as a dopant by a hydrothermal method. The second part was the synthesis of N-ZnO with urea as the nitrogen dopant carried out by a calcination method in a furnace at 500 °C for 2 h in an N2 atmosphere (5 °C min-1). The third part was the synthesis of N-ZnO/CD nanocomposites. The characteristics of CDs, N-ZnO, and N-ZnO/CD nanocomposites were analyzed through Fourier transform infrared (FTIR), UV-vis absorbance, photoluminescence (PL), high-resolution transmission electron microscopy (HR-TEM), X-ray diffraction (XRD), thermal gravimetry analysis (TGA), field-emission scanning electron microscopy energy-dispersive spectroscopy (FESEM EDS), X-ray photoelectron spectroscopy (XPS), and Brunauer-Emmett-Teller (BET) analysis. Based on the HR-TEM analysis, the CDs had a spherical shape with an average particle size of 4.249 nm. Meanwhile, based on the XRD and HR-TEM characterization, the N-ZnO and N-ZnO/CD nanocomposites have wurtzite hexagonal structures. The materials of N-ZnO and N-ZnO/CD show increased adsorption in the visible light region and low energy gap E g. The E g values of N-ZnO and N-ZnO/CDs were found to be 2.95 and 2.81 eV, respectively, whereas the surface area (S BET) values 3.827 m2 g-1 (N-ZnO) and 3.757 m2 g-1(N-ZnO/CDs) belonged to the microporous structure. In the last part, the photocatalysts of CDs, N-ZnO, and N-ZnO/CD nanocomposites were used for degradation of MB (10 ppm) under UV-B light irradiation pH = 7.04 (neutral) for 60 min at room temperature. The N-ZnO/CD nanocomposites showed a photodegradation efficiency of 83.4% with a kinetic rate of 0.0299 min-1 higher than N-ZnO and CDs. The XRD analysis and FESEM EDS of the N-ZnO/CDs before and after three cycles confirm the stability of the photocatalyst with an MB degradation of 58.2%. These results have clearly shown that the N-ZnO/CD nanocomposites could be used as an ideal photocatalytic material for the decolorization of organic compounds in wastewater.

Conformal Noble Metal High-Entropy Alloy Nanofilms by Atomic Layer Deposition for an Enhanced Hydrogen Evolution Reaction.

The current synthesis methods of high-entropy alloy (HEA) thin-film coatings face huge challenges in facile preparation, precise thickness control, conformal integration, and affordability. These challenges are more specific and noteworthy for noble metal-based HEA thin films where the conventional sputtering methods encounter thickness control and high-cost issues (high-purity noble metal targets required). Herein, for the first time, we report a facile and controllable synthesis process of quinary HEA coatings consisting of noble metals (Rh, Ru, Pt, Pd, and Ir), by sequential atomic layer deposition (ALD) coupled with electrical Joule heating for post-alloying. Furthermore, the resulting quinary HEA thin film with a thickness of ∼50 nm and an atomic ratio of 20:15:21:18:27 shows promising potential as a platform for catalysis, exhibiting enhanced electrocatalytic hydrogen evolution reaction (HER) performances with lower overpotentials (e.g., from 85 to 58 mV in 0.5 M H2SO4) and higher stability (by retaining more than 92% of the initial current after 20 h with a current density of 10 mA/cm2 in 0.5 M H2SO4) than other noble metal-based structure counterparts in this work. The enhanced material properties and device performances are attributed to the efficient electron transfer of HEA with the increased number of active sites. This work not only presents RhRuPtPdIr HEA thin films as promising HER catalysts but also sheds light on controllable fabrication of conformal HEA-coated complex structures toward a broad range of applications.

The New Materials for Battery Electrode Prototypes.

In this article, we present the performance of Copper (Cu)/Graphene Nano Sheets (GNS) and C-π (Graphite, GNS, and Nitrogen-doped Graphene Nano Sheets (N-GNS)) as a new battery electrode prototype. The objectives of this research are to develop a number of prototypes of the battery electrode, namely Cu/GNS//Electrolyte//C-π, and to evaluate their respective performances. The GNS, N-GNS, and primary battery electrode prototypes (Cu/GNS/Electrolyte/C-π) were synthesized by using a modified Hummers method; the N-doped sheet was obtained by doping nitrogen at room temperature and the impregnation or the composite techniques, respectively. Commercial primary battery electrodes were also used as a reference in this research. The Graphite, GNS, N-GNS, commercial primary batteries electrode, and battery electrode prototypes were analyzed using an XRD, SEM-EDX, and electrical multimeter, respectively. The research data show that the Cu particles are well deposited on the GNS and N-GNS (XRD and SEM-EDX data). The presence of the Cu metal and electrolytes (NH4Cl and MnO2) materials can increase the electrical conductivities (335.6 S cm-1) and power density versus the energy density (4640.47 W kg-1 and 2557.55 Wh kg-1) of the Cu/GNS//Electrolyte//N-GNS compared to the commercial battery (electrical conductivity (902.2 S cm-1) and power density versus the energy density (76 W kg-1 and 43.95 W kg-1). Based on all of the research data, it may be concluded that Cu/GNS//Electrolyte//N-GNS can be used as a new battery electrode prototype with better performances and electrical activities.

Sustainable Production of Molybdenum Carbide (MXene) from Fruit Wastes for Improved Solar Evaporation.

Invited for the cover of this issue is the group of Edison Huixiang Ang at the National Institute of Education, an institute of Nanyang Technological University, Singapore. The image depicts the sustainable fabrication of two-dimensional MXene sheets from the upcycling of fruit waste for solar desalination. Read the full text of the article at 10.1002/chem.202203184.

Affimer sandwich probes for stable and robust lateral flow assaying.

Lateral flow assays (LFAs) widely deployed for on-site diagnosis have predominantly utilized antibodies as recognition molecules. Antibodies with limited thermal stability deteriorate the performance of the LFA over time. Herein, we demonstrate a stable and robust LFA by utilizing thermally stable peptide-based 12-14 kDa affimers as recognition molecules, in lieu of conventional protein-based antibodies to analyze complex samples with a significantly improved shelf life at room temperature. The model system studied here is that of interleukin-8 (IL8) biomarker for validating the efficacy of the proposed approach, using a pair of affimer probes that demonstrates dual functionality of capturing and reporting. Affimers immobilized on the test zone of LFA serve as capture probes for IL8-affimer-MB complexes. Whereas affimers conjugated with the MBs that enable extraction of IL8 from the sample matrix serve as reporters for visual detection. The MB complexes captured at the test zone resulted in brownish test bands that enable concentration-dependent detection of IL8. The assay yielded sensitive visual detection of IL8 at ng/mL levels (~ 0.1 ng/mL and 1 ng/mL in buffer and human plasma, respectively), within 20 min, using sample volumes of ~ 100 µL. Importantly, the stability of affimer-incorporated LFA improved significantly in contrast to antibody-incorporated LFA over time, even when stored at 4 °C. Therefore, the proposed affimer-based LFA in conjunction with MBs offer stable and reliable detection of biomarkers at clinically relevant concentration ranges in complicated matrices, even without requiring cold storage, hence, offering a promising avenue for on-site diagnosis in resource-limited settings.

Noble metal alloy thin films by atomic layer deposition and rapid Joule heating.

Metal alloys are usually fabricated by melting constituent metals together or sintering metal alloy particles made by high energy ball milling (mechanical alloying). All these methods only allow for bulk alloys to be formed. This manuscript details a new method of fabricating Rhodium-Iridium (Rh-Ir) metal alloy films using atomic layer deposition (ALD) and rapid Joule heating induced alloying that gives functional thin film alloys, enabling conformal thin films with high aspect ratios on 3D nanostructured substrate. In this work, ALD was used to deposit Rh thin film on an Al2O3 substrate, followed by an Ir overlayer on top of the Rh film. The multilayered structure was then alloyed/sintered using rapid Joule heating. We can precisely control the thickness of the resultant alloy films down to the atomic scale. The Rh-Ir alloy thin films were characterized using scanning and transmission electron microscopy (SEM/TEM) and energy dispersive spectroscopy (EDS) to study their microstructural characteristics which showed the morphology difference before and after rapid Joule heating and confirmed the interdiffusion between Rh and Ir during rapid Joule heating. The diffraction peak shift was observed by Grazing-incidence X-ray diffraction (GIXRD) indicating the formation of Rh-Ir thin film alloys after rapid Joule heating. X-ray photoelectron spectroscopy (XPS) was also carried out and implied the formation of Rh-Ir alloy. Molecular dynamics simulation experiments of Rh-Ir alloys using Large-Scale Atomic/Molecular Massively Parallel Simulator (LAMMPS) were performed to elucidate the alloying mechanism during the rapid heating process, corroborating the experimental results.

Mechanically Durable Memristor Arrays Based on a Discrete Structure Design.

Memristors constitute a promising functional component for information storage and in-memory computing in flexible and stretchable electronics including wearable devices, prosthetics, and soft robotics. Despite tremendous efforts made to adapt conventional rigid memristors to flexible and stretchable scenarios, stretchable and mechanical-damage-endurable memristors, which are critical for maintaining reliable functions under unexpected mechanical attack, have never been achieved. Here, the development of stretchable memristors with mechanical damage endurance based on a discrete structure design is reported. The memristors possess large stretchability (40%) and excellent deformability (half-fold), and retain stable performances under dynamic stretching and releasing. It is shown that the memristors maintain reliable functions and preserve information after extreme mechanical damage, including puncture (up to 100 times) and serious tearing situations (fully diagonally cut). The structural strategy offers new opportunities for next-generation stretchable memristors with mechanical damage endurance, which is vital to achieve reliable functions for flexible and stretchable electronics even in extreme and highly dynamic environments.

Inorganic Photonic Microspheres with Localized Concentric Ordering for Deep Pattern Encoding and Triple Sensory Microsensor.

Photonic microspheres offer building units with unique topological structures and specific optical functions for diverse applications. Here, a new class of inorganic photonic microspheres with superior robustness, optical and electrical properties is reported by introducing a unique localized concentric ordering architecture and chemical interaction, which further serve as building blocks for deep pattern encoding and multiple sensory optoelectronic devices. Benefiting from localized concentric ordering architecture, the resultant photonic microspheres demonstrate orientation- and angle-independent structural colors. Notably, the formation of well-combined lamellae inorganic layers by chemical interaction grants the microspheres superior mechanical robustness, excellent solvent resistance, thermal stability, and multiple optoelectronic properties simultaneously, rarely seen in previous reports. Owing to these merits, such microspheres are used to construct diverse encoded photonic patterns for anti-counterfeiting applications. Interestingly, cross-communication among neighboring microspheres creates complex photonic sub-patterns, which provide "fingerprint information" with deep encryption security. Moreover, a single photonic microsphere-based optoelectronic microsensor is demonstrated for the first time, which achieves appealing application for real-time health monitoring and safety warning toward triple environmental stimuli. This work not only provides a new kind of robust, multifunctional photonic material, but also opens a new avenue for their uses as complexed pattern encoding and multi-parametric sensing platforms.

Periodic FTO IOs/CdS NRs/CdSe Clusters with Superior Light Scattering Ability for Improved Photoelectrochemical Performance.

Periodic fluorine-doped tin oxide inverse opals (FTO IOs) grafted with CdS nanorods (NRs) and CdSe clusters are reported for improved photoelectrochemical (PEC) performance. This hierarchical photoanode is fabricated by a combination of dip-coating, hydrothermal reaction, and chemical bath deposition. The growth of 1D CdS NRs on the periodic walls of 3D FTO IOs forms a unique 3D/1D hierarchical structure, providing a sizeable specific surface area for the loading of CdSe clusters. Significantly, the periodic FTO IOs enable uniform light scattering while the abundant surrounded CdS NRs induce additional random light scattering, combining to give multiple light scattering within the complete hierarchical structure, significantly improving light-harvesting of CdS NRs and CdSe clusters. The high electron collection ability of FTO IOs and the CdS/CdSe heterojunction formation also contribute to the enhanced charge transport and separation. Due to the incorporation of these enhancement strategies in one hierarchical structure, FTO IOs/CdS NRs/CdSe clusters present an improved PEC performance. The photocurrent density of FTO IOs/CdS NRs/CdSe clusters at 1.23 V versus reversible hydrogen electrode reaches 9.2 mA cm-2 , which is 1.43 times greater than that of CdS NRs/CdSe clusters and 3.83 times of CdS NRs.

Self-Assembled VO2 Mesh Film-Based Resistance Switches with High Transparency and Abrupt ON/OFF Ratio.

Vanadium dioxide, a well-known phase transition material with abrupt resistance change during its transition temperature, is herein used to fabricate the transparent mesh film onto a glass slide through self-assembly mesh printing. A record high ON/OFF ratio up to 104 is achieved together with high visible transmittance of 86% compared to the normal glass slide with visible transmittance at 88%. The high transparent properties make the resistive switches applicable for next-generation electronics, such as see-through computing device and beyond. A simple and scalable mesh printing approach-integrated phase change material may provide a promising way to fabricate transparent resistance switches for next-generation electronics.

Additive-Free Electrophoretic Deposition of Graphene Quantum Dots Thin Films.

The electrophoretic deposition (EPD) of graphene-based materials on transparent substrates is highly potential for many applications. Several factors can determine the yield of the EPD process, such as applied voltage, deposition time and particularly the presence of dispersion additives (stabilisers) in the suspension solution. This study presents an additive-free EPD of graphene quantum dot (GQD) thin films on an indium tin oxide (ITO) glass substrate and studies the deposition mechanism with the variation of the applied voltage (10-50 V) and deposition time (5-25 min). It is found that due to the small size (≈3.9 nm) and high content of deprotonated carboxylic groups, the GQDs form a stable dispersion (zeta-potential of about -35 mV) without using additives. The GQD thin films can be deposited onto ITO with optimal surface morphology at 30 V in 5 min (surface roughness of approximately (3.1±1.3) nm). In addition, as-fabricated GQD thin films also possess some interesting physico-optical properties, such as a double-peak photoluminescence at about λ=417 and 439 nm, with approximately 98 % visible transmittance. This low-cost and eco-friendly GQD thin film is a promising material for various applications, for example, transparent conductors, supercapacitors and heat conductive films in smart windows.

Multicolored Photonic Crystal Carbon Fiber Yarns and Fabrics with Mechanical Robustness for Thermal Management.

Multicolored photonic crystal carbon fiber (CF) yarns and fabrics with mechanical robustness in a full spectrum are reported. By facilely controlling the thickness of the periodic layer, a series of photonic CF yarns and fabrics with vivid structural colors ranging from purple, green, yellow, orange, to red are obtained. Interestingly, the prepared multicolored CF yarns show anisotropic optical reflection properties because of their unique axisymmetric geometry, while the plain-woven fabrics exhibit vivid colors even under ambient scattering light. Most importantly, they can withstand cyclical mechanical rubbing, laundering, and accelerated light aging, indicating great potential for practical uses. Finally, considering such impressive characteristics as well as reflection in the visible and near-infrared regions, the above photonic crystal microstructure is further used as a new material for the application of outdoor reflective cooling of the textile surface, demonstrating a superior temperature reduction up to ∼12 °C with respect to the control sample.

3D FTO/FTO-Nanocrystal/TiO2 Composite Inverse Opal Photoanode for Efficient Photoelectrochemical Water Splitting.

A 3D fluorine-doped SnO2 (FTO)/FTO-nanocrystal (NC)/TiO2 inverse opal (IO) structure is designed and fabricated as a new "host and guest" type of composite photoanode for efficient photoelectrochemical (PEC) water splitting. In this novel photoanode design, the highly conductive and porous FTO/FTO-NC IO acts as the "host" skeleton, which provides direct pathways for faster electron transport, while the conformally coated TiO2 layer acts as the "guest" absorber layer. The unique composite IO structure is fabricated through self-assembly of colloidal spheres template, a hydrothermal method and atomic layer deposition (ALD). Owing to its large surface area and efficient charge collection, the FTO/FTO-NC/TiO2 composite IO photoanode shows excellent photocatalytic properties for PEC water splitting. With optimized dimensions of the SnO2 nanocrystals and the thickness of the ALD TiO2 absorber layers, the 3D FTO/FTO-NC/TiO2 composite IO photoanode yields a photocurrent density of 1.0 mA cm-2 at 1.23 V versus reversible hydrogen electrode (RHE) under AM 1.5 illumination, which is four times higher than that of the FTO/TiO2 IO reference photoanode.

Supercompressible Coaxial Carbon Nanotube@Graphene Arrays with Invariant Viscoelasticity over -100 to 500 °C in Ambient Air.

Vertically aligned carbon nanotube (CNT) arrays have been recognized as promising cushion materials because of their superior thermal stability, remarkable compressibility, and viscoelastic characteristics. However, most of the previously reported CNT arrays still suffer from permanent shape deformation at only moderate compressive strains, which considerably restricts their practical applications. Here, we demonstrate a facile strategy of fabricating supercompressible coaxial CNT@graphene (CNT@Gr) arrays by using a two-step route involving encapsulating polymer layers onto plastic CNT arrays and subsequent annealing processes. Notably, the resulting CNT@Gr arrays are able to almost completely recover from compression at a strain of up to 80% and retain ∼80% recovery even after 1000 compression cycles at a 60% strain, demonstrating their excellent compressibility. Furthermore, they possess outstanding strain- and frequency-dependent viscoelastic responses, with storage modulus and damping ratio of up to ∼6.5 MPa and ∼0.19, respectively, which are nearly constant over an exceptionally broad temperature range of -100 to 500 °C in ambient air. These supercompressibility and temperature-invariant viscoelasticity together with facile fabrication process of the CNT@Gr arrays enable their promising multifunctional applications such as energy absorbers, mechanical sensors, and heat exchangers, even in extreme environments.

Development of a chemiluminescent DNA fibre optic genosensor to Hepatitis A Virus (HAV).

Hepatitis A virus (HAV) infection has caused substantial morbidity and economic losses to human society, presenting a major public health problem in many parts of the world. Despite the capability for low-concentration detection, current PCR-based techniques are limited by the requirement of specialized lab equipment, trained personnel and a relatively large time-commitment. The need for a prompt in-field quantitative identification of HAV in real samples has led us to develop a chemiluminescent fibre optic genosensor system. In this study, a two-probe sandwich-type hybridization process was implemented on the tip of a fibre optic with an area of 0.12mm2. After optimization of the probes and the working conditions, we showed that the biosensor was able to work for both cDNA and RNA with a relatively large signal/noise ratio and a good sensitivity. An excellent specificity was also confirmed by screening with a broad range of other pathogen samples. The nucleic acid probes method was validated by optimized PCR and qPCR, and may thus be used when field testing would be required.

Thermal Conductivity Enhancement of Coaxial Carbon@Boron Nitride Nanotube Arrays.

We demonstrate the thermal conductivity enhancement of the vertically aligned carbon nanotube (CNT) arrays (from ∼15.5 to 29.5 W/mK, ∼90% increase) by encapsulating outer boron nitride nanotube (BNNT, 0.97 nm-thick with ∼3-4 walls). The heat transfer enhancement mechanism of the coaxial C@BNNT was further revealed by molecular dynamics simulations. Because of their highly coherent lattice structures, the outer BNNT serves as additional heat conducting path without impairing the thermal conductance of inner CNT. This work provides deep insights into tailoring the heat transfer of arbitrary CNT arrays and will enable their broader applications as thermal interface material.

Biocompatible Hydroxylated Boron Nitride Nanosheets/Poly(vinyl alcohol) Interpenetrating Hydrogels with Enhanced Mechanical and Thermal Responses.

Poly(vinyl alcohol) (PVA) hydrogels with tissue-like viscoelasticity, excellent biocompatibility, and high hydrophilicity have been considered as promising cartilage replacement materials. However, lack of sufficient mechanical properties is a critical barrier to their use as load-bearing cartilage substitutes. Herein, we report hydroxylated boron nitride nanosheets (OH-BNNS)/PVA interpenetrating hydrogels by cyclically freezing/thawing the aqueous mixture of PVA and highly hydrophilic OH-BNNS (up to 0.6 mg/mL, two times the highest reported so far). Encouragingly, the resulting OH-BNNS/PVA hydrogels exhibit controllable reinforcements in both mechanical and thermal responses by simply varying the OH-BNNS contents. Impressive 45, 43, and 63% increases in compressive, tensile strengths and Young's modulus, respectively, can be obtained even with only 0.12 wt% (OH-BNNS:PVA) OH-BNNS addition. Meanwhile, exciting improvements in the thermal diffusivity (15%) and conductivity (5%) can also be successfully achieved. These enhancements are attributed to the synergistic effect of intrinsic superior properties of the as-prepared OH-BNNS and strong hydrogen bonding interactions between the OH-BNNS and PVA chains. In addition, excellent cytocompatibility of the composite hydrogels was verified by cell proliferation and live/dead viability assays. These biocompatible OH-BNNS/PVA hydrogels are promising in addressing the mechanical failure and locally overheating issues as cartilage substitutes and may also have broad utility for biomedical applications, such as drug delivery, tissue engineering, biosensors, and actuators.

Two-Dimensional SiO2/VO2 Photonic Crystals with Statically Visible and Dynamically Infrared Modulated for Smart Window Deployment.

Two-dimensional (2D) photonic structures, widely used for generating photonic band gaps (PBG) in a variety of materials, are for the first time integrated with the temperature-dependent phase change of vanadium dioxide (VO2). VO2 possesses thermochromic properties, whose potential remains unrealized due to an undesirable yellow-brown color. Here, a SiO2/VO2 core/shell 2D photonic crystal is demonstrated to exhibit static visible light tunability and dynamic near-infrared (NIR) modulation. Three-dimensional (3D) finite difference time domain (FDTD) simulations predict that the transmittance can be tuned across the visible spectrum, while maintaining good solar regulation efficiency (ΔTsol = 11.0%) and high solar transmittance (Tlum = 49.6%). Experiments show that the color changes of VO2 films are accompanied by NIR modulation. This work presents a novel way to manipulate VO2 photonic structures to modulate light transmission as a function of wavelength at different temperatures.